Canonical Allele Identifier: CA2624250773
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431028_23431029del , CM000676.2:g.23431028_23431029del GRCh38
NC_000014.8:g.23900237_23900238del , CM000676.1:g.23900237_23900238del GRCh37
NC_000014.7:g.22970077_22970078del NCBI36
NG_007884.1:g.9637_9638del , LRG_384:g.9637_9638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-26_797-25del MANE Select ENSP00000347507.3:n.797-26_797-25del
ENST00000355349.3:c.797-26_797-25del ENSP00000347507.3:n.797-26_797-25del
NM_000257.3:c.797-26_797-25del NP_000248.2:n.797-26_797-25del
XR_245686.3:n.903-26_903-25del
XM_017021340.1:c.797-26_797-25del XP_016876829.1:n.797-26_797-25del
NM_000257.4:c.797-26_797-25del MANE Select NP_000248.2:n.797-26_797-25del